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黄芪提取物对结肠腺癌Caco-2细胞葡萄糖吸收的影响
引用本文:张磊,曾丹,郑媛嘉,许燕玲,郭文峰.黄芪提取物对结肠腺癌Caco-2细胞葡萄糖吸收的影响[J].中国实验方剂学杂志,2016,22(24):145-149.
作者姓名:张磊  曾丹  郑媛嘉  许燕玲  郭文峰
作者单位:广州中医药大学 脾胃研究所, 广州 510405,广州中医药大学 脾胃研究所, 广州 510405,广州中医药大学 脾胃研究所, 广州 510405,广州中医药大学 脾胃研究所, 广州 510405,广州中医药大学 脾胃研究所, 广州 510405
基金项目:国家自然科学基金项目(81072753)
摘    要:目的:探讨黄芪提取物对Caco-2细胞葡萄糖吸收的影响,并探讨其作用机制。方法:采用系统溶剂法提取黄芪各部位,以Caco-2细胞为研究对象,设立空白组和黄芪各提取部位组(乙醇、石油醚、乙酸乙酯、正丁醇4个部位组)。以荧光标记2-脱氧葡萄糖(2-NBDG)做为光学探针检测黄芪各提取部位对Caco-2细胞葡萄糖吸收能力的影响。筛选出黄芪中促进Caco-2细胞葡萄糖吸收的药效部位后,对这一药效部位有效作用浓度进行考察。采用蛋白免疫印迹法(Western blot)法测定Caco-2细胞钠依赖葡萄糖转运蛋白(SGLT1)和2型葡萄糖转运蛋白(GLUT2)蛋白表达。结果:黄芪正丁醇提取部位可以促进Caco-2细胞葡萄糖的吸收,与空白组比较,黄芪正丁醇提取部位100,150 mg·L-1组Caco-2细胞葡萄糖含量升高(P0.05,P0.01);且黄芪正丁醇部位可以上调Caco-2细胞GLUT2和SGLT1蛋白的表达(P0.05,P0.01)。结论:黄芪正丁醇萃取部位可以促进Caco-2细胞葡萄糖的吸收,这一作用机制可能与SGLT1和GLUT2蛋白的调节有关。

关 键 词:黄芪  Caco-2细胞  葡萄糖吸收  钠依赖葡萄糖转运蛋白  2型葡萄糖转运蛋白
收稿时间:3/1/2016 12:00:00 AM

Effect of Astragali Radix Extracts on Glucose Absorption in Colon Adenocarcinoma Caco-2 Cell
ZHANG Lei,ZENG Dan,ZHENG Yuan-ji,XU Yan-ling and GUO Wen-feng.Effect of Astragali Radix Extracts on Glucose Absorption in Colon Adenocarcinoma Caco-2 Cell[J].China Journal of Experimental Traditional Medical Formulae,2016,22(24):145-149.
Authors:ZHANG Lei  ZENG Dan  ZHENG Yuan-ji  XU Yan-ling and GUO Wen-feng
Institution:Gastroenterology Research Institute, Guangzhou University of Chinese Medicine, Guangzhou 510405, China,Gastroenterology Research Institute, Guangzhou University of Chinese Medicine, Guangzhou 510405, China,Gastroenterology Research Institute, Guangzhou University of Chinese Medicine, Guangzhou 510405, China,Gastroenterology Research Institute, Guangzhou University of Chinese Medicine, Guangzhou 510405, China and Gastroenterology Research Institute, Guangzhou University of Chinese Medicine, Guangzhou 510405, China
Abstract:Objective: To investigate effects of Astragali Radix extracts on glucose absorption in Caco-2 cell and its relevant regulation mechanism. Method: All extracts of Astragali Radix were extracted by using systematical solvent separation method. Except for the blank group, Caco-2 cells were treated with Astragali Radix extracts, and then divided into four extraction groups (ethanol, petroleum ether, ethyl acetate, and n-butanol). The glucose absorption was detected by using the fluorescent D-glucose analog, with 2-deoxyglucose (2-NBDG) as the probe indicator. After the efficient extracts for promoting glucose absorption in Caco-2 cell was extracted from Astragali Radix, its effective concentration was studied. The expression of sodium-dependent glucose transporter 1 (SGLT1) and glucose transporter 2 (GLUT2) were detected by Western blot. Result: Astragali Radix n-butanol extract could improve glucose absorption in Caco-2 cell. Compared with control group, Astragali Radix n-butanol extract 100, 150 mg·L-1 group showed significant increase in glucose content in Caco-2 cells (P<0.05, P<0.01). N-butyl alcohol extracts of Astragali Radix could up-regulate GLUT2 and SGLT1 of Caco-2 cells (P<0.05, P<0.01). Conclusion: Astragali Radix n-butanol extract can promote the glucose absorption in Caco-2 cells. Its mechanism of improving glucose absorption may be correlated with regulation of SGLT1 and GLUT2.
Keywords:Astragali Radix  Caco-2 cell  glucose absorption  sodium-dependent glucose transporter 1 (SGLT1)  glucose transporter 2 (GLUT2)
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